Smiths Medical recalls ENT RES 100 ML Non-Sterile Medication Cassette Reservoirs with weak weld joints that could cause medication leakage. Product code 68-2230-28, specific lot numbers listed. No remedy provided in recall notice.
Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.
Smiths Medical is recalling ENT RES 100 ML Non-Sterile Medication Cassette Reservoirs that may have a weakened weld joint, potentially causing medication leakage. This could lead to improper medication delivery if the reservoir leaks.
The product may have a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could cause medication leakage, which might lead to improper medication delivery if the reservoir leaks.
Patients using this specific medical device for medication delivery are affected. Healthcare providers who use the product for clinical purposes are most at risk.
Check for the product code 68-2230-28 on the device. Look for specific lot numbers listed in the recall notice, which include many combinations starting with '4010559AB' through '4183674AB'.
Identify the product code (68-2230-28) and lot numbers listed in the recall notice to confirm if your device is affected.
The recall notice does not provide a remedy; the official notice states the remedy is null.
The recall states that medication leakage could occur, potentially leading to improper medication delivery.
Check for the product code 68-2230-28 and specific lot numbers listed in the recall notice, which include many combinations starting with '4010559AB' through '4183674AB'.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0017-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0017-2025 from Smiths Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
